FDA recalls 1-gallon Kill 'Dat hand sanitizer due to acetaldehyde levels exceeding specifications. Consumers should check batch numbers and contact the manufacturer for details.
CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.
Lula Holdings recalls 1-gallon hand sanitizer products containing 80% alcohol because FDA testing found acetaldehyde levels above acceptable limits. This could pose a risk of irritation or other health effects if used improperly.
The hand sanitizer contains acetaldehyde levels above what the FDA allows. Acetaldehyde is a chemical that can cause skin irritation or allergic reactions in some people, especially those with sensitive skin or allergies.
Anyone who purchased the 1-gallon hand sanitizer with batch number 39 from the manufacturer's website or retail stores. People with sensitive skin or allergies may be at higher risk.
Check the product label for 'Kill 'Dat Sanitizing Products Hand Sanitizer, 1 gallon (128 fl. oz.) 80% Alcohol' and batch number 39. The product was manufactured by Lula Holdings LLC in New Orleans, LA.
Look for the batch number 39 on the label to confirm if the product is recalled.
The FDA found acetaldehyde levels above specifications, which could cause skin irritation or allergic reactions in some people. The product is not safe for those with sensitive skin or allergies.
Check the product label for 'Kill 'Dat Sanitizing Products Hand Sanitizer, 1 gallon (128 fl. oz.) 80% Alcohol' and batch number 39.
The recall does not include a specific remedy, so you should check the product label for batch number 39 and contact the manufacturer if you have concerns.
We’ve drafted a message you can send Kill 'Dat to request your refund or repair — edit it as you like.
Subject: Recall D-0859-2022 — Kill 'Dat Kill 'Dat Hello, I own a Kill 'Dat that is covered by recall D-0859-2022 from Kill 'Dat. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
